Clinical Investigator

The Clinical Research Monitor / CRA / Site Monitor will coordinate clinical studies and shall be responsible for study execution, monitoring, site-training and close-out. - Coordinating site selection, contract negotiation, IRB/EC submissions, study initiation, monitoring, and site close-out. - Liaising and maintaining relationships with investigators, site...

Optum is a global organization that delivers care aided by technology to help millions of people live healthier lives The work you do with our team will directly improve health outcomes by connecting people with the care pharmacy benefits data and resources they need to feel their best Here you will find a culture guided by inclusion talented peers...

**Position Description**: Responsibilities may include the following and other duties may be assigned. - Monitors progress of clinical trials at the site level or headquarters and ensures that they are conducted, recorded and reported in accordance with the protocol, standard operating procedures (SOP), good clinical practices (GCP), and other applicable...

Summary:The Senior Quality Complaints Investigator I is responsible for performing and aiding in complaints investigations as well as product performance, complaint reporting to regulatory agencies and trend analysis activities.Responsibilities:Maintain complete and accurate complaint records. Evaluate the potential risks associated with customer complaints...

Job DescriptionThe role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our company's policies and procedures, quality standards and adverse event reporting requirements internally and...

Job DescriptionThe role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our company's policies and procedures, quality standards and adverse event reporting requirements internally and...

We are currently looking for passionate, and committed professional to join our team as Research associates. B. Pharm, M. Pharm preferred or Bachelor's Degree in a Life Sciences discipline or health care, with Post Graduate Diploma in clinical research. The ideal profile will have 0.5- 2 years of experience. An equivalent combination of education, training...

Job DescriptionThe role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our company's policies and procedures, quality standards and adverse event reporting requirements internally and...

**Description** **Principal Safety & Pharmacovigilance Specialist** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide...

Project Director Stem cell therapy projectGurgaon, IndiaPermanent roleQualifications:PhD (minimum) inStem cell biologyTissue engineeringBiomedical SciencesOrMD in relevant field with Postdoctoral training in stem cell research or regenerative medicine (preferred)Preferred (not essential): MBA or PMP certificationExperience & Skill set required:8-10 years +...